Cutter

GUDID 08437006085434

NEOS SURGERY SL

General internal orthopaedic fixation system implantation kit
Primary Device ID08437006085434
NIH Device Record Keya1c8c128-ba31-4d56-8eec-5a09a0e00d88
Commercial Distribution StatusIn Commercial Distribution
Brand NameCutter
Version Model NumberSCI0700
Company DUNS465890437
Company NameNEOS SURGERY SL
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone0935944726
Emailinfo@neosurgery.com
Phone0935944726
Emailinfo@neosurgery.com
Phone0935944726
Emailinfo@neosurgery.com
Phone0935944726
Emailinfo@neosurgery.com
Phone0935944726
Emailinfo@neosurgery.com
Phone0935944726
Emailinfo@neosurgery.com
Phone0935944726
Emailinfo@neosurgery.com
Phone0935944726
Emailinfo@neosurgery.com
Phone0935944726
Emailinfo@neosurgery.com
Phone0935944726
Emailinfo@neosurgery.com
Phone0935944726
Emailinfo@neosurgery.com

Device Identifiers

Device Issuing AgencyDevice ID
GS108437006085434 [Primary]

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08437006085434]

Moist Heat or Steam Sterilization


[08437006085434]

Moist Heat or Steam Sterilization


[08437006085434]

Moist Heat or Steam Sterilization


[08437006085434]

Moist Heat or Steam Sterilization


[08437006085434]

Moist Heat or Steam Sterilization


[08437006085434]

Moist Heat or Steam Sterilization


[08437006085434]

Moist Heat or Steam Sterilization


[08437006085434]

Moist Heat or Steam Sterilization


[08437006085434]

Moist Heat or Steam Sterilization


[08437006085434]

Moist Heat or Steam Sterilization


[08437006085434]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-09-12
Device Publish Date2024-09-04

Devices Manufactured by NEOS SURGERY SL

08437006085182 - Depth Gauge2024-09-12 DEPTH GAUGE
08437006085212 - Retractor2024-09-12
08437006085434 - Cutter2024-09-12
08437006085434 - Cutter2024-09-12
28437006085452 - STERN FIX2024-09-12 STERN FIX Sternal Stabilization System, Size 2
28437006085469 - STERN FIX2024-09-12 STERN FIX Sternal Stabilization System- size 3
08437006085472 - STERN FIX2024-09-12 STERN FIX Sternal Stabilization System-Size 4
28437006085483 - STERN FIX2024-09-12 STERN FIX Sternal Stabilization System- Size 5
08437006085496 - Forceps2024-09-12

Trademark Results [Cutter]

Mark Image

Registration | Serial
Company
Trademark
Application Date
CUTTER
CUTTER
97820387 not registered Live/Pending
United Industries Corporation
2023-03-02
CUTTER
CUTTER
97564943 not registered Live/Pending
Global Tobacco, LLC
2022-08-25
CUTTER
CUTTER
97305519 not registered Live/Pending
Linzer Products Corp.
2022-03-10
CUTTER
CUTTER
90532872 not registered Live/Pending
United Industries Corporation
2021-02-17
CUTTER
CUTTER
90502340 not registered Live/Pending
United Industries Corporation
2021-02-01
CUTTER
CUTTER
90502311 not registered Live/Pending
United Industries Corporation
2021-02-01
CUTTER
CUTTER
90212930 not registered Live/Pending
United Industries Corporation
2020-09-26
CUTTER
CUTTER
88886942 not registered Live/Pending
United Industries Corporation
2020-04-24
CUTTER
CUTTER
87226981 not registered Dead/Abandoned
United Industries Corporation
2016-11-04
CUTTER
CUTTER
86501045 5453846 Live/Registered
United Industries Corporation
2015-01-12
CUTTER
CUTTER
86306302 not registered Dead/Abandoned
United Industries Corporation
2014-06-11
CUTTER
CUTTER
86088498 4521956 Live/Registered
United Industries Corporation
2013-10-10

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